Metal Oxide Sandwiches: New option to manipulate properties of interfaces

Sketch of the structure of both metal oxide layers. Interesting new properties can arise at the interface.

Sketch of the structure of both metal oxide layers. Interesting new properties can arise at the interface. © M.Bibes

A Franco-German cooperation has investigated a sandwich system of transition metal oxides at BESSY II. The scientists discovered a new option to control properties of the interface between the two layers, for instance the amount of charge transferred from one layer to the other or the emergence of ferromagnetism.  Their insights might help to create new properties at the interface, not present in the primary materials, maybe even novel forms of High Tc superconductivity.

Sandwich systems of thin film transition metal oxides display surprising properties at their interfaces. In case of the paradigmatic example of Lanthan-Aluminate ( LaAlO3) and Strontium-Titanate (SrTiO3) both materials are insulators and non-magnetic, while their interface has been observed to display ferromagnetism, high electrical conductivity and even superconductivity.

Now the team of Manuel Bibes, CNRS Thales at Palaiseau, France, in collaboration with scientists at HZB around Sergio Valencia and several European groups, devised a new approach to tailor interface properties. Together they designed a series of experiments at the synchrotron source BESSY II to shed more light on the emergence of such property changes, identifying a new “knob” for their control.

Rare-Earth Elements influence charge transfer

The samples, which the team of Manuel Bibes did produce, consisted of a sandwich of 2 nm  Gadolinium-Titanate (GdTiO3) and “R”-Nickelate (RNiO3) films, where R is a rare-earth element. “We have been able to combine two very different transition metal oxides: whereas in the titanate electrons in the chemical bonds are strongly localized around the ions, in the nickelate side these electrons are shared between Nickel- and Oxygen-ions, and thus highly covalent”, Manuel Bibes explains. When putting both materials together some charge is transferred from the titanate layer to the nickelate one. They investigated this charge transfer process for samples containing different rare-earth elements in the nickelate layer such as Lanthanum, Neodymium and Samarium at BESSY II.

Their results show that the charge transfer at the interface between the materials strongly depends on the rare earth element in the nickelate layer. Different rare-earth elements have different atomic radii (size).This modifies the interaction between the Ni and O atoms and the degree of “covalency” between Ni and O changes. This was already known, but now the scientists have observed that this also affects the charge transferred from the GdTiO3 to the Nickelate film. “This is the key result”, Sergio Valencia from HZB explains. “We have found a new “knob”. Covalency (which is controlled by changing R) controls the charge transfer between the titanate and the nickelate.”

Ferromagnetism observed, superconductivity still searched

Tuning the charge transfer in this way might allow to control the formation of new interfacial phases too. For example, the scientists observed a new ferromagnetic phase at the interface. “Our work may help in the ongoing quest for cuprate-like superconductivity in nickelate heterostructures”, Valencia says. “We hope that this study will help to design better interfaces for exploring new exciting new phases of matter at interfaces between covalent materials”, Bibes adds.

Published in Nature Physics: doi:10.1038/nphys3627
'Hybridization-controlled charge transfer and induced magnetism at correlated oxide interfaces' . M. N. Grisolia, J. Varignon, G. Sanchez-Santolino, A. Arora, S. Valencia, M. Varela, R. Abrudan, E.Weschke, E. Schierle, J. E. Rault, J.-P. Rueff, A. Barthélémy, J. Santamaria and M. Bibes

arö

  • Copy link

You might also be interested in

  • Porous Radical Organic framework improves lithium-sulphur batteries
    Science Highlight
    15.09.2025
    Porous Radical Organic framework improves lithium-sulphur batteries
    A team led by Prof. Yan Lu, HZB, and Prof. Arne Thomas, Technical University of Berlin, has developed a material that enhances the capacity and stability of lithium-sulphur batteries. The material is based on polymers that form a framework with open pores (known as radical-cationic covalent organic frameworks or COFs). Catalytically accelerated reactions take place in these pores, firmly trapping polysulphides, which would shorten the battery life. Some of the experimental analyses were conducted at the BAMline at BESSY II.
  • Metallic nanocatalysts: what really happens during catalysis
    Science Highlight
    10.09.2025
    Metallic nanocatalysts: what really happens during catalysis
    Using a combination of spectromicroscopy at BESSY II and microscopic analyses at DESY's NanoLab, a team has gained new insights into the chemical behaviour of nanocatalysts during catalysis. The nanoparticles consisted of a platinum core with a rhodium shell. This configuration allows a better understanding of structural changes in, for example, rhodium-platinum catalysts for emission control. The results show that under typical catalytic conditions, some of the rhodium in the shell can diffuse into the interior of the nanoparticles. However, most of it remains on the surface and oxidises. This process is strongly dependent on the surface orientation of the nanoparticle facets.
  • Shedding light on insulators: how light pulses unfreeze electrons
    Science Highlight
    08.09.2025
    Shedding light on insulators: how light pulses unfreeze electrons
    Metal oxides are abundant in nature and central to technologies such as photocatalysis and photovoltaics. Yet, many suffer from poor electrical conduction, caused by strong repulsion between electrons in neighboring metal atoms. Researchers at HZB and partner institutions have shown that light pulses can temporarily weaken these repulsive forces, lowering the energy required for electrons mobility, inducing a metal-like behavior. This discovery offers a new way to manipulate material properties with light, with high potential to more efficient light-based devices.